Cytotoxicity of aqueous and ethanolic extracts of ficus deltoidea on human ovarian carcinoma cell line

Aims: This study was to investigate the cytotoxicity of both plant extracts from Ficus deltoidea (locally known as Mas Cotek), aqueous and ethanolic extracts on human ovarian carcinoma cells using standard colometric MTT assay. Study design: Cell based assay Place and Duration of Study: Institute of...

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Main Authors: Mat Akhir, Nor Azurah, Lee, Suan Chua, Abdul Majid, Fadzilah Adibah, Sarmidi, Mohamad Roji
Format: Article
Published: Sciencedomain international (SDI) 2011
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Online Access:http://eprints.utm.my/id/eprint/39799/
http://dx.doi.org/10.9734/BJMMR/2011/507
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spelling my.utm.397992019-03-17T04:02:19Z http://eprints.utm.my/id/eprint/39799/ Cytotoxicity of aqueous and ethanolic extracts of ficus deltoidea on human ovarian carcinoma cell line Mat Akhir, Nor Azurah Lee, Suan Chua Abdul Majid, Fadzilah Adibah Sarmidi, Mohamad Roji QD Chemistry Aims: This study was to investigate the cytotoxicity of both plant extracts from Ficus deltoidea (locally known as Mas Cotek), aqueous and ethanolic extracts on human ovarian carcinoma cells using standard colometric MTT assay. Study design: Cell based assay Place and Duration of Study: Institute of Bioproduct Development and Department of Bioprocess Engineering, Universiti Teknologi Malaysia, Johor Bahru, Malayisa between January 2007 and December 2009. Methodology: The biochemical responses of cells after plant sample treatment were observed and have been reported through several assays such as trypan blue exclusion assay for cell viability, analysis of glucose uptake and lactate release, cell survival evaluation and genomic assay through DNA fragmentation. Results: Both aqueous and ethanolic extracts of the plant sample gave IC50 value of 224.39 + 6.24 µg/ml and 143.03 ± 20.21 µg/ml, respectively. The detachment capability of the plant aqueous extract was observed in the cell viability assays. DNA fragmentation was not observed in the aqueous extract, but in ethanolic extract (1000 µg/ml). The DNA was fragmented around 200 Kbp. Morphological observation was carried out and apoptosis body was observed at 1000 µg/ml of both extract. Conclusion: A2780 cancer cells behaved differently on cell growth profile upon treating with different concentrations of the aquoues and ethanolic extracts of F. deltoidea. Even though both extracts could cause apoptosis at 1000 µg/ml, the aqueous extract prompted to promote cell detachment, and the ethanolic tried to inhibit cell proliferation through DNA fragmentation. Sciencedomain international (SDI) 2011-10 Article PeerReviewed Mat Akhir, Nor Azurah and Lee, Suan Chua and Abdul Majid, Fadzilah Adibah and Sarmidi, Mohamad Roji (2011) Cytotoxicity of aqueous and ethanolic extracts of ficus deltoidea on human ovarian carcinoma cell line. British Journal of Medicine & Medical Research, 1 (4). pp. 397-409. ISSN 2231-0614 http://dx.doi.org/10.9734/BJMMR/2011/507 DOI:10.9734/BJMMR/2011/507
institution Universiti Teknologi Malaysia
building UTM Library
collection Institutional Repository
continent Asia
country Malaysia
content_provider Universiti Teknologi Malaysia
content_source UTM Institutional Repository
url_provider http://eprints.utm.my/
topic QD Chemistry
spellingShingle QD Chemistry
Mat Akhir, Nor Azurah
Lee, Suan Chua
Abdul Majid, Fadzilah Adibah
Sarmidi, Mohamad Roji
Cytotoxicity of aqueous and ethanolic extracts of ficus deltoidea on human ovarian carcinoma cell line
description Aims: This study was to investigate the cytotoxicity of both plant extracts from Ficus deltoidea (locally known as Mas Cotek), aqueous and ethanolic extracts on human ovarian carcinoma cells using standard colometric MTT assay. Study design: Cell based assay Place and Duration of Study: Institute of Bioproduct Development and Department of Bioprocess Engineering, Universiti Teknologi Malaysia, Johor Bahru, Malayisa between January 2007 and December 2009. Methodology: The biochemical responses of cells after plant sample treatment were observed and have been reported through several assays such as trypan blue exclusion assay for cell viability, analysis of glucose uptake and lactate release, cell survival evaluation and genomic assay through DNA fragmentation. Results: Both aqueous and ethanolic extracts of the plant sample gave IC50 value of 224.39 + 6.24 µg/ml and 143.03 ± 20.21 µg/ml, respectively. The detachment capability of the plant aqueous extract was observed in the cell viability assays. DNA fragmentation was not observed in the aqueous extract, but in ethanolic extract (1000 µg/ml). The DNA was fragmented around 200 Kbp. Morphological observation was carried out and apoptosis body was observed at 1000 µg/ml of both extract. Conclusion: A2780 cancer cells behaved differently on cell growth profile upon treating with different concentrations of the aquoues and ethanolic extracts of F. deltoidea. Even though both extracts could cause apoptosis at 1000 µg/ml, the aqueous extract prompted to promote cell detachment, and the ethanolic tried to inhibit cell proliferation through DNA fragmentation.
format Article
author Mat Akhir, Nor Azurah
Lee, Suan Chua
Abdul Majid, Fadzilah Adibah
Sarmidi, Mohamad Roji
author_facet Mat Akhir, Nor Azurah
Lee, Suan Chua
Abdul Majid, Fadzilah Adibah
Sarmidi, Mohamad Roji
author_sort Mat Akhir, Nor Azurah
title Cytotoxicity of aqueous and ethanolic extracts of ficus deltoidea on human ovarian carcinoma cell line
title_short Cytotoxicity of aqueous and ethanolic extracts of ficus deltoidea on human ovarian carcinoma cell line
title_full Cytotoxicity of aqueous and ethanolic extracts of ficus deltoidea on human ovarian carcinoma cell line
title_fullStr Cytotoxicity of aqueous and ethanolic extracts of ficus deltoidea on human ovarian carcinoma cell line
title_full_unstemmed Cytotoxicity of aqueous and ethanolic extracts of ficus deltoidea on human ovarian carcinoma cell line
title_sort cytotoxicity of aqueous and ethanolic extracts of ficus deltoidea on human ovarian carcinoma cell line
publisher Sciencedomain international (SDI)
publishDate 2011
url http://eprints.utm.my/id/eprint/39799/
http://dx.doi.org/10.9734/BJMMR/2011/507
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